K250325
- 510(k) number
- K250325
- Device name
- BD Alaris Pump Infusion Set
- Applicant
- Carefusion (Bd) CA · US
- Product code
- FPA — Set, Administration, Intravascular
- Decision date
- 2025-10-30
- Date received
- 2025-02-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K250325.pdf
Official FDA record: K250325
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.